Effect of Core Stability Exercises and Russian Electrical Stimulation in Non-specific Low Back Pain

June 24, 2025 updated by: Deraya University

Effect of Core Stability Exercises and Russian Electrical Stimulation in Non-specific Low Back Pain (Randomized Control Trail)

Brief Summary: Low back pain (LBP) is an important public health problem due to the increasing world population and aging. In chronic LBP, exercise therapy is among the first-line treatments. Core stabilization exercises (CSE), one of the motor control exercises, focus on the activation and control of the deep spinal muscles. Recently, some studies have shown that Russian electrical stimulation alone or combined with exercise can provide contraction in deep stabilizer muscles and significantly reduce pain in patients with LBP

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Minya, Egypt, 05673
        • Deraya university

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • The duration of the disease is more than 3 months with pain scores greater than four in the VAS disability score of 19% or greater as evident from the modified oswestry disability.

Exclusion Criteria:

  • Neurological or musculoskeletal diseases that affect lumbar spine (e.g: lumbar spondylosis, spondylolisthesis, and lumbar disc injuries)
  • women during pregnancy and lactation.
  • History of lumbar spine surgery.
  • Signs of lumbar radiculopathy or myelopathy.
  • Signs of serious pathology (e.g., malignancy, inflammatory disorders, infection

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: group A
The training group A will be treated by core stability exercises and Russian electrical stimulation
Type of Medium frequency current with 2500 Hz frequency modulated at 50 Hz with 50% Duty cycle training protocol is (10 sec. on time - 50 sec. off time - 10 minutes total time)
Active Comparator: group B
The training group B will be treated by core stability exercises.
Type of Medium frequency current with 2500 Hz frequency modulated at 50 Hz with 50% Duty cycle training protocol is (10 sec. on time - 50 sec. off time - 10 minutes total time)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain scoring
Time Frame: 6 weeks
pain measured by VAS tool, 0 the least pain while 10 the highest one
6 weeks
Quality of life by using Oswestry Disability Index (OID)
Time Frame: 6 weeks
questioner, Score from 0 to 19% indicate minimal disability- 20 to 39% represent moderate disability- 40 to 59% represent severe disability- 60 to 79% represent crippled disability- and scores from 80 to 100% represents patients that are confined to bed
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle thickness assessment
Time Frame: 6 weeks
Ultrasonography
6 weeks
Stability and mobility of spine
Time Frame: 6 weeks
Spinal mouse assessment spinal vertebrate from 7th cervical vertebrae to 3rd sacral vertebrae
6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 10, 2024

Primary Completion (Actual)

June 30, 2024

Study Completion (Actual)

July 31, 2024

Study Registration Dates

First Submitted

July 2, 2024

First Submitted That Met QC Criteria

July 2, 2024

First Posted (Actual)

July 10, 2024

Study Record Updates

Last Update Posted (Actual)

June 26, 2025

Last Update Submitted That Met QC Criteria

June 24, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • physio 224

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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